meddevicedb.com FDA Device Reference

LSF(TM) TOTAL HIP SYSTEM

K901460 Class II Traditional
Decision Date
1990-05-22
Sponsor / Applicant
Implant Technology, Inc.

Technical Specification

510(k) Submission ID K901460
Product Code JDI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3350
Decision Date 1990-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LSF(TM) TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K901460, sponsored by Implant Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.